Acetate → HCID 22064679, compound

HRID 1828104Notes

Reaction equation

HRID 1828104 reaction equation
[CH2:1]([O:3][CH:4]([N:8]1[CH2:16][C:15]2[C:10](=[CH:11][CH:12]=[CH:13][C:14]=2[CH3:17])[C:9]1=[O:18])[C:5]([OH:7])=O)[CH3:2].C([O-])(=O)C.[NH2:23][CH2:24][C:25]1[CH:32]=[CH:31][C:28]([C:29]#[N:30])=[CH:27][C:26]=1[N+:33]([O-:35])=[O:34]>>[C:29]([C:28]1[CH:31]=[CH:32][C:25]([CH2:24][NH:23][C:5](=[O:7])[CH:4]([O:3][CH2:1][CH3:2])[N:8]2[CH2:16][C:15]3[C:10](=[CH:11][CH:12]=[CH:13][C:14]=3[CH3:17])[C:9]2=[O:18])=[C:26]([N+:33]([O-:35])=[O:34])[CH:27]=1)#[N:30]

Participants

4

Reactant 3

HCID 175AcetateHCID 21905720HCID 21905720, compoundHCID 22064727α-Ethoxy-1,3-dihydro-4-methyl-1-oxo-2H-isoindole-2-acetic acid

Product 1

HCID 22064679HCID 22064679, compound

Procedure

According to general procedure C, (RS)-ethoxy-(4-methyl-1-oxo-1,3-dihydro-isoindol-2-yl)-acetic acid (intermediate of example 44) was coupled with 4-aminomethyl-3-nitrobenzonitrile (CAS 701269-65-0) to give (RS)-N-(4-cyano-2-nitro-benzyl)-2-ethoxy-2-(4-methyl-1-oxo-1,3-dihydro-isoindol-2-yl)-acetamide as off-white crystals, MS 409.4 ([M+H]+).

Sources & evidence

ORD record
ord-0d14fdd7d3284b1ca31df3e25481180b
Source dataset
uspto-grants-2006_06
Patent number
US07056932B2

Reaction notes

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